Canonical Allele Identifier: CA1969379712

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47449086G= , CM000673.2:g.47449086G=	GRCh38
NC_000011.9:g.47470638G= , CM000673.1:g.47470638G=	GRCh37
NC_000011.8:g.47427214G=	NCBI36
NG_008312.1:g.5093C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.-122C= MANE Select	ENSP00000298854.2:n.-122C=
ENST00000298854.6:c.-122C=	ENSP00000298854.2:n.-122C=
ENST00000352508.7:c.-122C=	ENSP00000298853.3:n.-122C=
ENST00000524487.5:c.-122C=	ENSP00000435551.2:n.-122C=
ENST00000529341.1:c.-122C=	ENSP00000431732.1:n.-122C=
NM_005055.4:c.-122C=	NP_005046.2:n.-122C=
NM_032645.4:c.-122C=	NP_116034.2:n.-122C=
XM_005253042.2:c.-122C=	XP_005253099.1:n.-122C=
XM_005253043.2:c.-122C=	XP_005253100.1:n.-122C=
XM_011520252.1:c.-122C=	XP_011518554.1:n.-122C=
XM_011520253.1:c.-122C=	XP_011518555.1:n.-122C=
XM_005253042.3:c.-122C=	XP_005253099.1:n.-122C=
XM_005253043.3:c.-122C=	XP_005253100.1:n.-122C=
NM_005055.5:c.-122C= MANE Select	NP_005046.2:n.-122C=
NM_032645.5:c.-122C=	NP_116034.2:n.-122C=